Canonical Allele Identifier: CA2379736620

Gene: TMPRSS15

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.18281024_18281025delinsGA , CM000683.2:g.18281024_18281025delinsGA	GRCh38
NC_000021.8:g.19653341_19653342delinsGA , CM000683.1:g.19653341_19653342delinsGA	GRCh37
NC_000021.7:g.18575212_18575213delinsGA	NCBI36
NG_012207.1:g.127629_127630delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284885.8:c.2668+15_2668+16delinsTC MANE Select	ENSP00000284885.3:n.2668+15_2668+16delinsTC
ENST00000284885.7:c.2668+15_2668+16delinsTC	ENSP00000284885.3:n.2668+15_2668+16delinsTC
NM_002772.2:c.2668+15_2668+16delinsTC	NP_002763.2:n.2668+15_2668+16delinsTC
XM_011529654.1:c.2803+15_2803+16delinsTC	XP_011527956.1:n.2803+15_2803+16delinsTC
XM_011529655.1:c.2803+15_2803+16delinsTC	XP_011527957.1:n.2803+15_2803+16delinsTC
XM_011529656.1:c.2803+15_2803+16delinsTC	XP_011527958.1:n.2803+15_2803+16delinsTC
XM_011529657.1:c.2758+15_2758+16delinsTC	XP_011527959.1:n.2758+15_2758+16delinsTC
XM_011529658.1:c.2722+15_2722+16delinsTC	XP_011527960.1:n.2722+15_2722+16delinsTC
XM_011529659.1:c.2713+15_2713+16delinsTC	XP_011527961.1:n.2713+15_2713+16delinsTC
XM_011529654.2:c.2803+15_2803+16delinsTC	XP_011527956.1:n.2803+15_2803+16delinsTC
XM_011529656.2:c.2803+15_2803+16delinsTC	XP_011527958.1:n.2803+15_2803+16delinsTC
XM_011529657.2:c.2758+15_2758+16delinsTC	XP_011527959.1:n.2758+15_2758+16delinsTC
XM_011529658.2:c.2722+15_2722+16delinsTC	XP_011527960.1:n.2722+15_2722+16delinsTC
NM_002772.3:c.2668+15_2668+16delinsTC MANE Select	NP_002763.3:n.2668+15_2668+16delinsTC